[Federal Register: May 25, 1999 (Volume 64, Number 100)]
[Notices]               
[Page 28214]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr25my99-104]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on March 2, 1999, Noramco, Inc., 
1400 Olympic Drive, Athens, Georgia 30601, made application to the Drug 
Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

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                    Drug                               Schedule
------------------------------------------------------------------------
Codeine (9050).............................  II
Oxycodone (9143)...........................  II
Hydrocodone (9193).........................  II
Morphine (9300)............................  II
Thebaine (9333)............................  II
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    The firm plans to support its other manufacturing facility with 
manufacturing and analytical testing.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substances may file comments or objections 
to the issuance of the proposed registration.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than July 26, 1999.

    Dated: May 12, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-13095 Filed 5-24-99; 8:45 am]
BILLING CODE 4410-09-M